Canonical Allele Identifier: PA132712
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43545
ClinVar RCV Id: RCV000036481 RCV000584878 RCV001164904 RCV001375368 RCV001164905 RCV004017307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Gly740Val
CA132711
NM_000441.2:c.2219G>T